Publication:
Longitudinal respiratory subphenotypes in patients with COVID-19-related acute respiratory distress syndrome: results from three observational cohorts

dc.contributor.authorLieuwe D.J. Bosen_US
dc.contributor.authorMichael Sjodingen_US
dc.contributor.authorPratik Sinhaen_US
dc.contributor.authorSivasubramanium V. Bhavanien_US
dc.contributor.authorPatrick G. Lyonsen_US
dc.contributor.authorAlice F. Bewleyen_US
dc.contributor.authorMichela Bottaen_US
dc.contributor.authorAnissa M. Tsonasen_US
dc.contributor.authorAry Serpa Netoen_US
dc.contributor.authorMarcus J. Schultzen_US
dc.contributor.authorRobert P. Dicksonen_US
dc.contributor.authorFrederique Paulusen_US
dc.contributor.authorJ. P. van Akkerenen_US
dc.contributor.authorA. G. Algeraen_US
dc.contributor.authorC. K. Algoeen_US
dc.contributor.authorR. B. van Amstelen_US
dc.contributor.authorA. Artigasen_US
dc.contributor.authorO. L. Bauren_US
dc.contributor.authorP. van de Bergen_US
dc.contributor.authorA. E. van den Bergen_US
dc.contributor.authorD. C.J.J. Bergmansen_US
dc.contributor.authorD. I. van den Bersselaaren_US
dc.contributor.authorF. A. Bertensen_US
dc.contributor.authorA. J.G.H. Bindelsen_US
dc.contributor.authorM. M. de Boeren_US
dc.contributor.authorS. den Boeren_US
dc.contributor.authorL. S. Boersen_US
dc.contributor.authorM. Bogerden_US
dc.contributor.authorL. D.J. Bosen_US
dc.contributor.authorJ. S. Breelen_US
dc.contributor.authorH. de Bruinen_US
dc.contributor.authorS. de Bruinen_US
dc.contributor.authorC. L. Brunaen_US
dc.contributor.authorL. A. Buiteman-Kruizingaen_US
dc.contributor.authorO. Cremeren_US
dc.contributor.authorR. M. Determannen_US
dc.contributor.authorW. Dieperinken_US
dc.contributor.authorD. A. Dongelmansen_US
dc.contributor.authorH. S. Frankeen_US
dc.contributor.authorM. S. Galek-Aldridgeen_US
dc.contributor.authorM. J. de Graaffen_US
dc.contributor.authorL. A. Hagensen_US
dc.contributor.authorJ. J. Haringmanen_US
dc.contributor.authorS. T. van der Heideen_US
dc.contributor.authorP. L.J. van der Heidenen_US
dc.contributor.authorN. F.L. Heijnenen_US
dc.contributor.authorS. J.P. Hielen_US
dc.contributor.authorL. L. Hoeijmakersen_US
dc.contributor.authorL. Holen_US
dc.contributor.authorM. W. Hollmannen_US
dc.contributor.authorM. E. Hoogendoornen_US
dc.contributor.authorJ. Hornen_US
dc.contributor.authorR. van der Horsten_US
dc.contributor.authorE. L.K. Ieen_US
dc.contributor.authorD. Ivanoven_US
dc.contributor.authorN. P. Juffermansen_US
dc.contributor.authorE. Khoen_US
dc.contributor.authorE. S. de Klerken_US
dc.contributor.authorA. W.M.M. Koopman-van Gemerten_US
dc.contributor.authorM. Koopmansen_US
dc.contributor.authorS. Kucukcelebien_US
dc.contributor.authorM. A. Kuiperen_US
dc.contributor.authorD. W. de Langeen_US
dc.contributor.authorI. Martin-Loechesen_US
dc.contributor.authorG. Mazzinarien_US
dc.contributor.authorD. M.P. van Meenenen_US
dc.contributor.authorL. Morales-Quinterosen_US
dc.contributor.authorN. van Mouriken_US
dc.contributor.authorS. G. Nijbroeken_US
dc.contributor.authorM. Onrusten_US
dc.contributor.authorE. A.N. Oostdijken_US
dc.contributor.authorF. Paulusen_US
dc.contributor.authorC. J. Pennartzen_US
dc.contributor.authorJ. Pillayen_US
dc.contributor.authorL. Pisanien_US
dc.contributor.authorI. M. Purmeren_US
dc.contributor.authorT. C.D. Rettigen_US
dc.contributor.authorJ. P. Roozemanen_US
dc.contributor.authorM. T.U. Schuijten_US
dc.contributor.authorM. J. Schultzen_US
dc.contributor.authorA. Serpa Netoen_US
dc.contributor.authorM. E. Sleeswijken_US
dc.contributor.authorM. R. Smiten_US
dc.contributor.authorP. E. Spronken_US
dc.contributor.authorW. Stilmaen_US
dc.contributor.authorA. C. Strangen_US
dc.contributor.authorP. R. Tuinmanen_US
dc.contributor.authorC. M.A. Valken_US
dc.contributor.authorF. L. Veen-Schraen_US
dc.contributor.authorL. I. Veldhuisen_US
dc.contributor.authorP. van Velzenen_US
dc.contributor.authorW. H. van der Venen_US
dc.contributor.authorA. P.J. Vlaaren_US
dc.contributor.authorP. van Vlieten_US
dc.contributor.authorP. H.J. van der Voorten_US
dc.contributor.authorL. van Welieen_US
dc.contributor.authorH. J.F.T. Wesselinken_US
dc.contributor.authorH. H. van der Wier-Lubbersen_US
dc.contributor.otherDepartment of Medicine, The University of Chicagoen_US
dc.contributor.otherUniversity of Melbourneen_US
dc.contributor.otherUniversity of Michigan, Ann Arboren_US
dc.contributor.otherWashington University School of Medicine in St. Louisen_US
dc.contributor.otherMonash Universityen_US
dc.contributor.otherHospital Israelita Albert Einsteinen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNuffield Department of Medicineen_US
dc.contributor.otherEmory Universityen_US
dc.contributor.otherAmsterdam UMCen_US
dc.date.accessioned2022-08-04T09:00:07Z
dc.date.available2022-08-04T09:00:07Z
dc.date.issued2021-12-01en_US
dc.description.abstractBackground: Patients with COVID-19-related acute respiratory distress syndrome (ARDS) have been postulated to present with distinct respiratory subphenotypes. However, most phenotyping schema have been limited by sample size, disregard for temporal dynamics, and insufficient validation. We aimed to identify respiratory subphenotypes of COVID-19-related ARDS using unbiased data-driven approaches. Methods: PRoVENT–COVID was an investigator-initiated, national, multicentre, prospective, observational cohort study at 22 intensive care units (ICUs) in the Netherlands. Consecutive patients who had received invasive mechanical ventilation for COVID-19 (aged 18 years or older) served as the derivation cohort, and similar patients from two ICUs in the USA served as the replication cohorts. COVID-19 was confirmed by positive RT-PCR. We used latent class analysis to identify subphenotypes using clinically available respiratory data cross-sectionally at baseline, and longitudinally using 8-hourly data from the first 4 days of invasive ventilation. We used group-based trajectory modelling to evaluate trajectories of individual variables and to facilitate potential clinical translation. The PRoVENT-COVID study is registered with ClinicalTrials.gov, NCT04346342. Findings: Between March 1, 2020, and May 15, 2020, 1007 patients were admitted to participating ICUs in the Netherlands, and included in the derivation cohort. Data for 288 patients were included in replication cohort 1 and 326 in replication cohort 2. Cross-sectional latent class analysis did not identify any underlying subphenotypes. Longitudinal latent class analysis identified two distinct subphenotypes. Subphenotype 2 was characterised by higher mechanical power, minute ventilation, and ventilatory ratio over the first 4 days of invasive mechanical ventilation than subphenotype 1, but PaO2/FiO2, pH, and compliance of the respiratory system did not differ between the two subphenotypes. 185 (28%) of 671 patients with subphenotype 1 and 109 (32%) of 336 patients with subphenotype 2 had died at day 28 (p=0·10). However, patients with subphenotype 2 had fewer ventilator-free days at day 28 (median 0, IQR 0–15 vs 5, 0–17; p=0·016) and more frequent venous thrombotic events (109 [32%] of 336 patients vs 176 [26%] of 671 patients; p=0·048) compared with subphenotype 1. Group-based trajectory modelling revealed trajectories of ventilatory ratio and mechanical power with similar dynamics to those observed in latent class analysis-derived trajectory subphenotypes. The two trajectories were: a stable value for ventilatory ratio or mechanical power over the first 4 days of invasive mechanical ventilation (trajectory A) or an upward trajectory (trajectory B). However, upward trajectories were better independent prognosticators for 28-day mortality (OR 1·64, 95% CI 1·17–2·29 for ventilatory ratio; 1·82, 1·24–2·66 for mechanical power). The association between upward ventilatory ratio trajectories (trajectory B) and 28-day mortality was confirmed in the replication cohorts (OR 4·65, 95% CI 1·87–11·6 for ventilatory ratio in replication cohort 1; 1·89, 1·05–3·37 for ventilatory ratio in replication cohort 2). Interpretation: At baseline, COVID-19-related ARDS has no consistent respiratory subphenotype. Patients diverged from a fairly homogenous to a more heterogeneous population, with trajectories of ventilatory ratio and mechanical power being the most discriminatory. Modelling these parameters alone provided prognostic value for duration of mechanical ventilation and mortality. Funding: Amsterdam UMC.en_US
dc.identifier.citationThe Lancet Respiratory Medicine. Vol.9, No.12 (2021), 1377-1386en_US
dc.identifier.doi10.1016/S2213-2600(21)00365-9en_US
dc.identifier.issn22132619en_US
dc.identifier.issn22132600en_US
dc.identifier.other2-s2.0-85120071049en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/77472
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85120071049&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleLongitudinal respiratory subphenotypes in patients with COVID-19-related acute respiratory distress syndrome: results from three observational cohortsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85120071049&origin=inwarden_US

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